ALLIUM- allium cepa tablet

ALLIUM by

Drug Labeling and Warnings

ALLIUM by is a Homeopathic medication manufactured, distributed, or labeled by STANDARD HOMEOPATHIC COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Made according to the
Homeopathic Pharmacopoeia
of the United States since 1903.

Warnings

Do not use if cap band is missing or broken.

If you are pregnant or nursing, consult a licensed health
care professional before using this product.

If symptoms persist for 7 days or worsen,
contact a licensed practitioner.

KEEP THIS AND ALL MEDICINES OUT OF THE REACH OF CHILDREN.

To be used according to label indications and/or
standard homeopathic indications.

QUESTIONS

Standard Homeopathic Company
Los Angeles, CA 90061
Questions? 800-624-9659

Directions

Adults: Dissolve 4 tablets under tongue 4 times a day.
Children: Consult a healthcare professional

INACTIVE INGREDIENT

In a base of Acacia Gum and Lactose N.F.

ACTIVE INGREDIENT

ALLIUM CEPA 6X

INDICATIONS & USAGE

RUNNY NOSE,COLD OR HAY FEVER

RUNNY NOSE,COLD OR HAY FEVER

Principal Display Panel -- 250 Tablet Bottle Label

Standard

Homeopathic

Made in the USA Since 1903

NDC # 0360-0015-01

Homeopathic Medicine

ALLIUM CEPA

6X

RUNNY NOSE,COLD OR HAY

FEVER*

*Claims based on traditional homeopathic

practice, not accepted medical evidence.

Not FDA evaluated.

250 TABLETS

INGREDIENTS AND APPEARANCE

ALLIUM 
allium cepa tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0360-0015
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLIUM CEPA WHOLE (UNII: 8P2VLG2456) (ALLIUM CEPA WHOLE - UNII:8P2VLG2456)	ALLIUM CEPA WHOLE	6 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ACACIA (UNII: 5C5403N26O)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	ROUND	Size	5mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0360-0015-01	1 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/17/1997

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/17/1997

Labeler - STANDARD HOMEOPATHIC COMPANY (008316655)

Establishment
Name	Address	ID/FEI	Business Operations
STANDARD HOMEOPATHIC COMPANY		008316655	pack(0360-0015) , manufacture(0360-0015) , label(0360-0015)